HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58098Generated: October 25, 2026
Sodium Bicarbonate → 3-(6-(trifluoromethyl)-1H-indazol-4-yl)benzenesulfonamide
https://huagongshe.com/reaction/58098
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Bromo-6-(trifluoromethyl)-1H-indazole | HCID 24729232 | — |
| Reactant | 3-(Aminosulphonyl)benzeneboronic acid | HCID 44119323 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(6-(trifluoromethyl)-1H-indazol-4-yl)benzenesulfonamide | HCID 89783011 | 69.5% |
Reaction Steps
4-Bromo-6-(trifluoromethyl)-1H-indazole (40 mg, 0.151 mmol), (3-sulfamoylphenyl)boronic acid (45.5 mg, 0.226 mmol), PdCl2(dppf) (11.04 mg, 0.015 mmol), sodium bicarbonate (323 μL, 0.604 mmol), and dioxane were mixed in a 10 mL vial to give an orange suspension. The vial was sealed and then heated to 140° C. for 20 minutes in a microwave reactor. The reaction mixture was subsequently filtered and the product was purified by preparative HPLC, eluting with a gradient of 35-70% ACN in H2O (containing 10 mM NH4HCO3). The pure fractions were lyophilized to give the title compound as a white solid (35.8 mg, 69.5%). 1H NMR (400 MHz, DMSO-d6) δ ppm 7.50 (s, 2H), 7.53 (s, 1H), 7.75-7.80 (m, 1H), 7.92-7.94 (m, 1H), 8.02 (s, 1H), 8.06 (dt, J=8.02, 1.29 Hz, 1H), 8.21 (t, J=1.64 Hz, 1H), 8.40 (s, 1H); ESI-MS m/z [M+H]+ calc'd for C14H10F3N3O2S, 342.0. found 342.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434743B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-367f38fb34bc4b4e8d6789a8dc992bd1 |
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| Source note | uspto-grants-2016_09 |
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